Canonical Allele Identifier: PA2828100870
Gene: MSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949625
ClinVar RCV Id: RCV002676357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Gly17Val
CA362229022
NM_001363626.2:c.50G>T